RS138925964 PROS1

Health Risk Chr 3:93879278 snv missense variant
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What This Variant Does
"rs138925964, also known as c.1528G&gt
Associated Conditions
Thrombophilia due to protein S deficiency
autosomal dominant
autosomal recessive
Protein S deficiency disease
PROS1-related disorder
Thrombophilia due to protein S deficiency
autosomal dominant
autosomal recessive
Protein S deficiency disease
PROS1-related disorder
Population Frequencies
gnomAD ALL
100%
1kG AFR
99.4%
1kG ALL
0.2%
1kG AMR
100%
1kG EAS
100%
1kG EUR
100%
1kG SAS
100%
Other Variants in PROS1
rs121918472 rs121918473 rs121918474 rs267606981 rs2107137679 rs121918475 rs387906674 rs387906675 rs142846443 rs199469491
Ask Dr. Hemsworth about this variant